Trials / Enrolling By Invitation
Enrolling By InvitationNCT07008469
Global Open-Label Extension Study of Del-desiran for the Treatment of DM1
A Global Phase 3 Open-Label Extension Study to Assess the Long-Term Safety, Tolerability, and Efficacy of Intravenous AOC 1001 for the Treatment of Myotonic Dystrophy Type 1
- Status
- Enrolling By Invitation
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 230 (estimated)
- Sponsor
- Avidity Biosciences, Inc. · Industry
- Sex
- All
- Age
- 16 Years
- Healthy volunteers
- Not accepted
Summary
A Global Phase 3 Open-Label Extension Study to Assess the Long-Term Safety, Tolerability, and Efficacy of Intravenous Delpacibart Etedesiran (abbreviated del-desiran, formerly AOC 1001) for the Treatment of Myotonic Dystrophy Type 1
Detailed description
The study consists of a Screening Period of up to either 4-weeks or 8-weeks depending on the prior parent trial, and up to a 4-year Treatment Period. The anticipated duration is 50 months and 2 weeks (4 years and 2.5 months). Participants will receive an intravenous infusion of del-desiran at the clinical study site every 8 weeks for a total of 7 doses per year. The final dose will occur at Year 4, Visit 7, followed by a final assessment 8 weeks after the last dose. An additional subgroup of de novo participants will also be included in a Fixed-Dose PK cohort. An Independent Data Monitoring Committee (IDMC) comprised of members independent and external to the Sponsor will review safety, tolerability, and efficacy (as needed) data of this study at regular intervals.
Conditions
- Myotonic Dystrophy Type 1
- DM1
- Myotonic Dystrophy
- Myotonia
- Myotonic Dystrophy 1
- Myotonic Disorders
- Steinert Myotonic Dystrophy
- Steinert Disease
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Del-desiran (AOC 1001) | Del-desiran will be administered by intravenous (IV) infusion. |
Timeline
- Start date
- 2025-07-25
- Primary completion
- 2030-08-01
- Completion
- 2030-10-01
- First posted
- 2025-06-06
- Last updated
- 2026-02-03
Locations
20 sites across 5 countries: United States, Canada, Italy, Japan, Netherlands
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT07008469. Inclusion in this directory is not an endorsement.